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AR078408A1 - DERIVATIVES OF INDOL AS MODULATORS OF THE CRAC - Google Patents

DERIVATIVES OF INDOL AS MODULATORS OF THE CRAC

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Publication number
AR078408A1
AR078408A1 ARP100103446A ARP100103446A AR078408A1 AR 078408 A1 AR078408 A1 AR 078408A1 AR P100103446 A ARP100103446 A AR P100103446A AR P100103446 A ARP100103446 A AR P100103446A AR 078408 A1 AR078408 A1 AR 078408A1
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AR
Argentina
Prior art keywords
alkyl
alkoxy
optionally substituted
phenyl
carbonyl
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Application number
ARP100103446A
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Spanish (es)
Inventor
Muzaffar Alam
Wylie Solang Palmer
Tania Silva
Robert Stephen Wilhelm
Ronald Charles Hawley
Joshua Kennedy-Smith
Ana Elena Minatti
Bois Daisy Joe Du
Original Assignee
Hoffmann La Roche
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Publication of AR078408A1 publication Critical patent/AR078408A1/en

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    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
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    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

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  • Physical Education & Sports Medicine (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)

Abstract

Se describen también métodos de obtencion de los compuestos y el uso de los compuestos para el tratamiento de enfermedades asociadas con los canales de calcio activados con la liberacion de calcio (CRAC). Reivindicacion 1: Un compuesto de la formula (1): en la que: R1 es: - fenilo sustituido una, dos o tres veces por un grupo o grupo elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; halo-alcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; aminocarbonilo; aminosulfonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; hidroxi; sulfonilmorfolina; sulfonilmetilpiperazina; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - piridinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6 nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - pirimidinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; o - un anillo heteroarilo de cinco eslabones opcionalmente sustituido una, dos o tres veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; cicloalquilo C3-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; y heteroarilo que puede estar opcionalmente sustituido; o dos de dichos sustituyentes junto con los átomos a los que están unidos pueden formar un fenilo fusionado con el anillo heteroarilo de cinco eslabones; es: - cicloalquilo C3-6; - fenilo sustituido una, dos o tres veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; alcoxihidroxi C1-6; halogeno; halo-alquilo C1-6; haloalcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; (alquil C1-6)-carbonilhidroxi; (alcoxi C1-6)-ciano; amino; hidroxi; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - piridinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonil- amino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - pirimidinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; o - un anillo heteroarilo de cinco eslabones opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; cicloalquilo C3-6; halo-alcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; fenilo que puede estar opcionalmente sustituido; y heteroarilo que puede estar opcionalmente sustituido; o dos de dichos sustituyentes junto con los átomos a los que están unidos pueden formar un fenilo fusionado con dicho anillo heteroarilo de cinco eslabones; R3 es hidrogeno; R3' es hidrogeno o alquilo C1-6; es un numero de 0 a 3; cada R4 se elige con independencia entre: hidrogeno; alquilo C1-6; alcoxi C1-6; halogeno; y halo-alquilo C1-6, y dicha línea discontinua es un enlace o está ausente, o una sal farmacéuticamente aceptable de los mismos.Methods of obtaining the compounds and the use of the compounds for the treatment of diseases associated with calcium channels activated with calcium release (CRAC) are also described. Claim 1: A compound of the formula (1): wherein: R1 is: - phenyl substituted once, twice or three times by a group or group independently selected from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; C1-6 haloalkoxy; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; aminocarbonyl; aminosulfonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; hydroxy; sulfonylmorpholine; sulfonylmethylpiperazine; heterocyclyl; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; - pyridinyl optionally substituted once or twice by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; halogen; halo-C1-6 alkyl nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; heterocyclyl; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; - pyrimidinyl optionally substituted once or twice by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; heterocyclyl; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; or - a five-link heteroaryl ring optionally substituted once, twice or three times by a group or groups chosen independently from: C1-6 alkyl; C3-6 cycloalkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; heterocyclyl; phenyl that may be optionally substituted; and heteroaryl which may be optionally substituted; or two of said substituents together with the atoms to which they are attached may form a phenyl fused with the five-link heteroaryl ring; is: - C3-6 cycloalkyl; - phenyl substituted once, twice or three times by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; C1-6 alkoxyhydroxy; halogen; halo C1-6 alkyl; C1-6 haloalkoxy; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; (C1-6 alkyl) -carbonylhydroxy; (C1-6 alkoxy) -cyano; Not me; hydroxy; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; - pyridinyl optionally substituted once or twice by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonyl-amino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; - pyrimidinyl optionally substituted once or twice by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; or - a five-link heteroaryl ring optionally substituted once or twice by a group or groups independently selected from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; C3-6 cycloalkyl; C1-6 haloalkoxy; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; phenyl that may be optionally substituted; and heteroaryl which may be optionally substituted; or two of said substituents together with the atoms to which they are attached may form a phenyl fused with said five-link heteroaryl ring; R3 is hydrogen; R3 'is hydrogen or C1-6 alkyl; it is a number from 0 to 3; each R4 is independently selected from: hydrogen; C1-6 alkyl; C1-6 alkoxy; halogen; and haloC 1-6 alkyl, and said broken line is a bond or is absent, or a pharmaceutically acceptable salt thereof.

ARP100103446A 2009-09-24 2010-09-22 DERIVATIVES OF INDOL AS MODULATORS OF THE CRAC AR078408A1 (en)

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US37806210P 2010-08-30 2010-08-30

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EP (1) EP2480529A1 (en)
JP (2) JP2013505913A (en)
KR (1) KR20120068947A (en)
CN (1) CN102574788A (en)
AR (1) AR078408A1 (en)
BR (1) BR112012006630A2 (en)
CA (1) CA2771026A1 (en)
MX (1) MX2012003539A (en)
RU (1) RU2012116207A (en)
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WO (1) WO2011036130A1 (en)

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